CAS 56-88-2|L-Cystathionine
| Common Name | L-Cystathionine | ||
|---|---|---|---|
| CAS Number | 56-88-2 | Molecular Weight | 222.262 |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 481.0±45.0 °C at 760 mmHg |
| Molecular Formula | C7H14N2O4S | Melting Point | 312ºC |
| MSDS | ChineseUSA | Flash Point | 244.7±28.7 °C |
Names
| Name | L-Cystathionine |
|---|---|
| Synonym | More Synonyms |
L-Cystathionine BiologicalActivity
| Description | L-Cystathionine is a key nonprotein amino acid related to metabolic conditions. |
|---|---|
| Related Catalog | Natural Products >>OthersResearch Areas >>Others |
| Target | Human Endogenous Metabolite |
| In Vitro | L-Cystathionine is an important metabolic intermediate in the L-cysteine transsulfuration pathway from L-methionine via L-homocysteine in mammalian tissues[1]. |
| References | [1]. Amino Y, et al. Synthesis and evaluation of L-cystathionine as a standard for amino acid analysis. Biosci Biotechnol Biochem. 2017 Jan;81(1):95-101. |
Chemical & Physical Properties
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 481.0±45.0 °C at 760 mmHg |
| Melting Point | 312ºC |
| Molecular Formula | C7H14N2O4S |
| Molecular Weight | 222.262 |
| Flash Point | 244.7±28.7 °C |
| Exact Mass | 222.067429 |
| PSA | 151.94000 |
| LogP | -0.13 |
| Vapour Pressure | 0.0±2.6 mmHg at 25°C |
| Index of Refraction | 1.592 |
| InChIKey | ILRYLPWNYFXEMH-WHFBIAKZSA-N |
| SMILES | NC(CCSCC(N)C(=O)O)C(=O)O |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
Articles63
More Articles| Physiology and pathophysiology of organic acids in cerebrospinal fluid. J. Inherit. Metab. Dis. 16(4) , 648-69, (1993) Concentrations of organic acids in cerebrospinal fluid (CSF) appear to be directly dependent upon their rate of production in the brain. There is evidence that the net release of short-chain monocarbo... | |
| Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression. Nature 457(7231) , 910-4, (2009) Multiple, complex molecular events characterize cancer development and progression. Deciphering the molecular networks that distinguish organ-confined disease from metastatic disease may lead to the i... | |
| Automated screening of urine samples for carbohydrates, organic and amino acids after treatment with urease. J. Chromatogr. A. 562(1-2) , 125-38, (1991) Eighty-five clinical urine samples and nineteen urine samples previously found by other laboratories to suggest genetic metabolic defects were prepared for trimethylsilylation by treatment with urease... |
Synonyms
| L-Cystathionine |
| EINECS 200-295-8 |
| D-Homocysteine, S-[(2R)-2-amino-2-carboxyethyl]- |
| L-2-Amino-4-[(2-amino-2-carboxyethyl)thio]butyric Acid |
| S-[(2R)-2-Amino-2-carboxyethyl]-D-homocysteine |
| (Quinoxalin-6-yl)methanamine hydrochloride |
| MFCD00036685 |
